Canonical Allele Identifier: CA660865633
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1391239135
gnomAD v3: 10-122461614-G-T
gnomAD v4: 10-122461614-G-T
MyVariant Identifiers: chr10:g.124221130G>T (hg19) chr10:g.122461614G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461614G>T , CM000672.2:g.122461614G>T GRCh38
NC_000010.10:g.124221130G>T , CM000672.1:g.124221130G>T GRCh37
NC_000010.9:g.124211120G>T NCBI36
NG_011554.1:g.5090G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.-39G>T MANE Select ENSP00000357980.3:n.-39G>T
ENST00000648167.1:c.154+2905G>T ENSP00000498033.1:n.154+2905G>T
ENST00000368984.7:c.-39G>T ENSP00000357980.3:n.-39G>T
NM_002775.4:c.-39G>T NP_002766.1:n.-39G>T
NM_002775.5:c.-39G>T MANE Select NP_002766.1:n.-39G>T
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